A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519626



Internal ID15100233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:103933493..104158390hg38UCSC Ensembl
InnerchrX:103188067..103403071hg19UCSC Ensembl
InnerchrX:103074723..103289727hg18UCSC Ensembl
InnerchrX:102994212..103209216hg17UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38224898
hg19215005
hg18215005
hg17215005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673366, nssv657215, nssv671922, nssv683117, nssv672582, nssv677802
Samples
Known GenesH2BFM, H2BFWT, H2BFXP, LOC286437, MIR1256, SLC25A53, TMSB15B, ZCCHC18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519626
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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